Topical Ruxolitinib in the Treatment of Necrobiosis Lipoidica: A Prospective, Open-Label Study.
Angelina S HwangJacob A KechterXing LiAlysia HughesKevin J SeversonBlake BoudreauxPuneet BhullarShams NassirMiranda YousifNan ZhangRichard J ButterfieldSteven NelsonXianying XingLam C TsoiSamantha ZunichAleksandar SekulicMark PittelkowJohann E GudjonssonAaron MangoldPublished in: The Journal of investigative dermatology (2024)
Necrobiosis lipoidica (NL) is a rare granulomatous disease. There are few effective treatments for NL. We sought to investigate the efficacy and safety of the Jak1/2 inhibitor, ruxolitnib, in the treatment of NL and identify the biomarkers associated with the disease and treatment response. We conducted an open-label, phase 2 study of ruxolitinib in 12 patients with NL. We performed transcriptomic analysis of tissue samples before and after treatment. At week 12, the mean NL lesion score decreased by 58.2% (SD = 28.7%, P = .003). Transcriptomic analysis demonstrated enrichment of type I and type II IFN pathways in baseline disease. Weighted gene coexpression network analysis demonstrated post-treatment changes in IFN pathways with key hub genes IFNG and signal transducer and activator of transcription 1 gene STAT1. Limitations include small sample size and a study group limited to patients with <10% body surface area. In conclusion, ruxolitinib is an effective treatment for NL and targets the key pathogenic mediators of the disease.
Keyphrases
- network analysis
- open label
- genome wide
- clinical trial
- transcription factor
- squamous cell carcinoma
- magnetic resonance imaging
- gene expression
- computed tomography
- dendritic cells
- rheumatoid arthritis
- cell proliferation
- copy number
- systemic sclerosis
- genome wide identification
- toll like receptor
- contrast enhanced
- genome wide analysis